colestid

Generic: colestipol hydrochloride

Labeler: pharmacia & upjohn company llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name colestid
Generic Name colestipol hydrochloride
Labeler pharmacia & upjohn company llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

colestipol hydrochloride 1 g/1

Manufacturer
Pharmacia & Upjohn Company LLC

Identifiers & Regulatory

Product NDC 0009-0450
Product ID 0009-0450_62a88ff5-632d-4fe7-a4e5-1170f1c70dd3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020222
Listing Expiration 2026-12-31
Marketing Start 1994-07-19

Pharmacologic Class

Classes
bile acid sequestrant [epc] bile-acid binding activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 00090450
Hyphenated Format 0009-0450

Supplemental Identifiers

RxCUI
1048445 1048447
UPC
0300090450038
UNII
X7D10K905G

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name colestid (source: ndc)
Generic Name colestipol hydrochloride (source: ndc)
Application Number NDA020222 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 120 TABLET in 1 BOTTLE (0009-0450-03)
source: ndc

Packages (1)

0009-0450-03 120 TABLET in 1 BOTTLE (0009-0450-03)

Ingredients (1)

colestipol hydrochloride (1 g/1)

Linked Drug Pages (1)

Colestid ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "62a88ff5-632d-4fe7-a4e5-1170f1c70dd3", "openfda": {"upc": ["0300090450038"], "unii": ["X7D10K905G"], "rxcui": ["1048445", "1048447"], "spl_set_id": ["3e270911-f27b-44d4-b0a2-33506418cc1d"], "manufacturer_name": ["Pharmacia & Upjohn Company LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (0009-0450-03)", "package_ndc": "0009-0450-03", "marketing_start_date": "19940719"}], "brand_name": "Colestid", "product_id": "0009-0450_62a88ff5-632d-4fe7-a4e5-1170f1c70dd3", "dosage_form": "TABLET", "pharm_class": ["Bile Acid Sequestrant [EPC]", "Bile-acid Binding Activity [MoA]"], "product_ndc": "0009-0450", "generic_name": "Colestipol Hydrochloride", "labeler_name": "Pharmacia & Upjohn Company LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Colestid", "active_ingredients": [{"name": "COLESTIPOL HYDROCHLORIDE", "strength": "1 g/1"}], "application_number": "NDA020222", "marketing_category": "NDA", "marketing_start_date": "19940719", "listing_expiration_date": "20261231"}